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Invitrogen™ GBA Polyclonal Antibody, Invitrogen™

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5145479
This item is not returnable.
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Description
GBA encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
Specifications
| GBA | |
| Polyclonal | |
| Unconjugated | |
| GBA | |
| acid beta glucosidase; acid beta-glucosidase; Alglucerase; betaGC; beta-GC; Beta-glucocerebrosidase; Cholesterol glucosyltransferase; Cholesteryl-beta-glucosidase; D-glucosyl-N-acylsphingosine glucohydrolase; Gba; GBA1; GBAP; GBAP1; GC; GCase; GCB; GLUC; glucocerebrosidase; glucosidase, beta, acid; glucosylceramidase; glucosylceramidase beta; glucosylceramidase beta pseudogene 1; glucosylceramidase-like protein; imiglucerase; Lysosomal acid GCase; Lysosomal acid glucosylceramidase; lysosomal glucocerebrosidase; SGTase | |
| Rabbit | |
| Antigen affinity chromatography, Protein A | |
| RUO | |
| 2629 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Western Blot, Immunohistochemistry (Paraffin), Western Blot | |
| 0.5 mg/mL | |
| PBS with 50% glycerol and 0.05% Proclin 300; pH 7.4 | |
| P04062 | |
| GBA | |
| Recombinant Human GBA protein, Ala40-Gln536 (Accession #P04062). | |
| 200 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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